메뉴 건너뛰기




Volumn 20, Issue 4, 1997, Pages 595-602

Plasma chitotriosidase activity in Gaucher disease patients who have been treated either by bone marrow transplantation or by enzyme replacement therapy with alglucerase

Author keywords

[No Author keywords available]

Indexed keywords

ALGLUCERASE; CHITINASE; PLACENTA ENZYME;

EID: 0030796039     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1005367328003     Document Type: Article
Times cited : (56)

References (14)
  • 1
    • 0025869216 scopus 로고
    • Replacement therapy for inherited enzyme deficiency-macrophage-targeted glucocerebrosidase for Gaucher's disease
    • Barton NW, Brady RO, Dambrosia JM, et al (1991) Replacement therapy for inherited enzyme deficiency-macrophage-targeted glucocerebrosidase for Gaucher's disease. N Engl J Med 324: 1464-1470.
    • (1991) N Engl J Med , vol.324 , pp. 1464-1470
    • Barton, N.W.1    Brady, R.O.2    Dambrosia, J.M.3
  • 4
    • 0029891549 scopus 로고    scopus 로고
    • Marked increase in methylumbelliferyl-tetra-N-acetyltetraoside hydrolase activity in plasma from Gaucher disease patients
    • Den Tandt WR, Van Hoof F (1996) Marked increase in methylumbelliferyl-tetra-N-acetyltetraoside hydrolase activity in plasma from Gaucher disease patients. J Inher Metab Dis 19: 344-350
    • (1996) J Inher Metab Dis , vol.19 , pp. 344-350
    • Den Tandt, W.R.1    Van Hoof, F.2
  • 5
    • 0028883136 scopus 로고
    • Enzyme therapy in Type 1 Gaucher disease: Comparative efficacy of mannose-terminated glucocerebrosidase from natural and recombinant sources
    • Grabowski GA, Barton NW, Pastores G, et al (1995) Enzyme therapy in Type 1 Gaucher disease: comparative efficacy of mannose-terminated glucocerebrosidase from natural and recombinant sources. Ann Intern Med 122: 33-39.
    • (1995) Ann Intern Med , vol.122 , pp. 33-39
    • Grabowski, G.A.1    Barton, N.W.2    Pastores, G.3
  • 6
    • 0029565165 scopus 로고
    • Elevated plasma chitotriosidase activity in various lysosomal storage disorders
    • Guo Y, He W, Boer Am, et al (1995) Elevated plasma chitotriosidase activity in various lysosomal storage disorders. J Inher Metab Dis 18: 717-722.
    • (1995) J Inher Metab Dis , vol.18 , pp. 717-722
    • Guo, Y.1    He, W.2    Boer, Am.3
  • 7
    • 0023221342 scopus 로고
    • Beneficial effects of pretransplant splenectomy on displacement bone marrow transplantation for Gaucher's disease
    • Hobbs JR, Hugh-Jones K, Shaw PJ, Lindsay I, Hancock M (1987) Beneficial effects of pretransplant splenectomy on displacement bone marrow transplantation for Gaucher's disease. Lancet i: 1111-1115.
    • (1987) Lancet , vol.1 , pp. 1111-1115
    • Hobbs, J.R.1    Hugh-Jones, K.2    Shaw, P.J.3    Lindsay, I.4    Hancock, M.5
  • 8
    • 0028220472 scopus 로고
    • Marked elevation of plasma chitotriosidase activity. A novel hallmark of Gaucher disease
    • Hollak CEM, van Weely S, van Oers MHJ, Aerts JMFG (1994) Marked elevation of plasma chitotriosidase activity. A novel hallmark of Gaucher disease. J Clin Invest 93: 1288-1292.
    • (1994) J Clin Invest , vol.93 , pp. 1288-1292
    • Hollak, C.E.M.1    Van Weely, S.2    Van Oers, M.H.J.3    Aerts, J.M.F.G.4
  • 9
    • 0029066515 scopus 로고
    • Individualised low-dose alglucerase therapy for Type 1 Gaucher's disease
    • Hollak CEM, Aerts JMFG, Goudsmit R, et al (1995) Individualised low-dose alglucerase therapy for Type 1 Gaucher's disease. Lancet 345: 1474-1478.
    • (1995) Lancet , vol.345 , pp. 1474-1478
    • Hollak, C.E.M.1    Aerts, J.M.F.G.2    Goudsmit, R.3
  • 10
    • 0027218354 scopus 로고
    • Enzyme therapy in Gaucher disease Type 1: Dosage efficacy and adverse effects in 33 patients treated for 6 to 24 months
    • Pastores GM, Sibille AR, Grabowski GA (1993) Enzyme therapy in Gaucher disease Type 1: dosage efficacy and adverse effects in 33 patients treated for 6 to 24 months. Blood 82: 408-416.
    • (1993) Blood , vol.82 , pp. 408-416
    • Pastores, G.M.1    Sibille, A.R.2    Grabowski, G.A.3
  • 11
    • 0028911536 scopus 로고
    • Purification and characterization of human chitotriosidase, a novel member of the chitinase family of proteins
    • Renkema GH, Boot RG, Muijsers AO, Donker-Koopman WE, Aerts JMFG (1995) Purification and characterization of human chitotriosidase, a novel member of the chitinase family of proteins. J Biol Chem 270: 2198-2202.
    • (1995) J Biol Chem , vol.270 , pp. 2198-2202
    • Renkema, G.H.1    Boot, R.G.2    Muijsers, A.O.3    Donker-Koopman, W.E.4    Aerts, J.M.F.G.5
  • 13
    • 0019059776 scopus 로고
    • Hydrolysis of 4-methylumbelliferyl-N-acetyl chitotetraoside catalyzed by lysozyme
    • Yang Y, Hamaguchi K (1980) Hydrolysis of 4-methylumbelliferyl-N-acetyl chitotetraoside catalyzed by lysozyme. J Biochem 88: 829-836.
    • (1980) J Biochem , vol.88 , pp. 829-836
    • Yang, Y.1    Hamaguchi, K.2
  • 14
    • 0028359980 scopus 로고
    • Low-dose enzyme replacement therapy for Gaucher disease: Effects of age, sex, genotype and clinical features on response to treatment
    • Zimran A, Elstein D, Kannai R, Zevin S, Hadas-Halpern I, Levy-Lahad E (1994) Low-dose enzyme replacement therapy for Gaucher disease: effects of age, sex, genotype and clinical features on response to treatment. Am J Med 97: 3-13.
    • (1994) Am J Med , vol.97 , pp. 3-13
    • Zimran, A.1    Elstein, D.2    Kannai, R.3    Zevin, S.4    Hadas-Halpern, I.5    Levy-Lahad, E.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.